Haplotype-aware diplotyping from noisy long reads

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1474-760X

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Haplotype-aware diplotyping from noisy long reads ; volume:20 ; number:1 ; day:3 ; month:6 ; year:2019 ; pages:1-16 ; date:12.2019
Genome biology ; 20, Heft 1 (3.6.2019), 1-16, 12.2019

Classification: Biowissenschaften, Biologie

Creator: Ebler, Jana
Haukness, Marina
Pesout, Trevor
Marschall, Tobias
Paten, Benedict

Contributor: SpringerLink (Online service)

DOI: 10.1186/s13059-019-1709-0

URN: urn:nbn:de:101:1-2019092323081437381240

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:20 AM CEST

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Ebler, Jana
Haukness, Marina
Pesout, Trevor
Marschall, Tobias
Paten, Benedict
SpringerLink (Online service)

Other Objects (12)

Strainline: full-length de novo viral haplotype reconstruction from noisy long reads

Computational Methods for Haplotype-aware De Novo Genome Assembly from Long Reads

phasebook: haplotype-aware de novo assembly of diploid genomes from long reads

Haplotype threading: accurate polyploid phasing from long reads

LRScaf: improving draft genomes using long noisy reads

Repeat and haplotype aware error correction in nanopore sequencing reads with DeChat

De novo diploid genome assembly using long noisy reads

Detecting haplotype-specific transcript variation in long reads with FLAIR2

MethPhaser: methylation-based long-read haplotype phasing of human genomes

Haplotype Inference Using Long-Read Nanopore Sequencing: Application to GSTA1 Promoter

S-conLSH: alignment-free gapped mapping of noisy long reads

Long-read sequencing identifies a common transposition haplotype predisposing for CLCNKB deletions

Strainline: full-length de novo viral haplotype reconstruction from noisy long reads

Computational Methods for Haplotype-aware De Novo Genome Assembly from Long Reads

phasebook: haplotype-aware de novo assembly of diploid genomes from long reads

Haplotype threading: accurate polyploid phasing from long reads

LRScaf: improving draft genomes using long noisy reads

Repeat and haplotype aware error correction in nanopore sequencing reads with DeChat

De novo diploid genome assembly using long noisy reads

Detecting haplotype-specific transcript variation in long reads with FLAIR2

MethPhaser: methylation-based long-read haplotype phasing of human genomes

Haplotype Inference Using Long-Read Nanopore Sequencing: Application to GSTA1 Promoter

S-conLSH: alignment-free gapped mapping of noisy long reads

Long-read sequencing identifies a common transposition haplotype predisposing for CLCNKB deletions

Strainline: full-length de novo viral haplotype reconstruction from noisy long reads

Computational Methods for Haplotype-aware De Novo Genome Assembly from Long Reads

phasebook: haplotype-aware de novo assembly of diploid genomes from long reads

Haplotype threading: accurate polyploid phasing from long reads

LRScaf: improving draft genomes using long noisy reads

Repeat and haplotype aware error correction in nanopore sequencing reads with DeChat

De novo diploid genome assembly using long noisy reads

Detecting haplotype-specific transcript variation in long reads with FLAIR2

MethPhaser: methylation-based long-read haplotype phasing of human genomes

Haplotype Inference Using Long-Read Nanopore Sequencing: Application to GSTA1 Promoter

S-conLSH: alignment-free gapped mapping of noisy long reads

Long-read sequencing identifies a common transposition haplotype predisposing for CLCNKB deletions

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Haplotype-aware diplotyping from noisy long reads

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Other Objects (12)

Strainline: full-length de novo viral haplotype reconstruction from noisy long reads

Computational Methods for Haplotype-aware De Novo Genome Assembly from Long Reads

phasebook: haplotype-aware de novo assembly of diploid genomes from long reads

Haplotype threading: accurate polyploid phasing from long reads

LRScaf: improving draft genomes using long noisy reads

Repeat and haplotype aware error correction in nanopore sequencing reads with DeChat

De novo diploid genome assembly using long noisy reads

Detecting haplotype-specific transcript variation in long reads with FLAIR2

MethPhaser: methylation-based long-read haplotype phasing of human genomes

Haplotype Inference Using Long-Read Nanopore Sequencing: Application to GSTA1 Promoter

S-conLSH: alignment-free gapped mapping of noisy long reads

Long-read sequencing identifies a common transposition haplotype predisposing for CLCNKB deletions

Strainline: full-length de novo viral haplotype reconstruction from noisy long reads

Computational Methods for Haplotype-aware De Novo Genome Assembly from Long Reads

phasebook: haplotype-aware de novo assembly of diploid genomes from long reads

Haplotype threading: accurate polyploid phasing from long reads

LRScaf: improving draft genomes using long noisy reads

Repeat and haplotype aware error correction in nanopore sequencing reads with DeChat

De novo diploid genome assembly using long noisy reads

Detecting haplotype-specific transcript variation in long reads with FLAIR2

MethPhaser: methylation-based long-read haplotype phasing of human genomes

Haplotype Inference Using Long-Read Nanopore Sequencing: Application to GSTA1 Promoter

S-conLSH: alignment-free gapped mapping of noisy long reads

Long-read sequencing identifies a common transposition haplotype predisposing for CLCNKB deletions

Strainline: full-length de novo viral haplotype reconstruction from noisy long reads

Computational Methods for Haplotype-aware De Novo Genome Assembly from Long Reads

phasebook: haplotype-aware de novo assembly of diploid genomes from long reads

Haplotype threading: accurate polyploid phasing from long reads

LRScaf: improving draft genomes using long noisy reads

Repeat and haplotype aware error correction in nanopore sequencing reads with DeChat

De novo diploid genome assembly using long noisy reads

Detecting haplotype-specific transcript variation in long reads with FLAIR2

MethPhaser: methylation-based long-read haplotype phasing of human genomes

Haplotype Inference Using Long-Read Nanopore Sequencing: Application to GSTA1 Promoter

S-conLSH: alignment-free gapped mapping of noisy long reads

Long-read sequencing identifies a common transposition haplotype predisposing for CLCNKB deletions

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